Inspiratory muscle training in children and adolescents living with neuromuscular diseases: A pre-experimental study

Anri Human, Brenda M Morrow, Anri Human, Brenda M Morrow

Abstract

Background: Children with neuromuscular diseases (NMD) are at risk of morbidity and mortality because of progressive respiratory muscle weakness and ineffective cough. Inspiratory muscle training (IMT) aims to preserve or improve respiratory muscle strength, thereby reducing morbidity and improving health-related quality of life (HRQoL).

Objectives: To describe the safety and feasibility of a 6-week IMT programme using an electronic threshold device (Powerbreathe®). Any adverse events and changes in functional ability, spirometry, peak expiratory cough flow (PECF), inspiratory muscle strength and HRQoL (Pediatric Quality of Life [PedsQL]) were recorded.

Methods: A convenience sample of eight participants (n = 4 boys; median [interquartile range {IQR}] age: 12.21 [9.63-16.05] years) with various NMD were included in a pre-experimental, observational pre-test post-test feasibility study. Training consisted of 30 breaths, twice daily, 5 days a week, for 6 weeks.

Results: There were significant pre- to post-intervention improvements in upper limb function and coordination (p = 0.03) and inspiratory muscle strength: maximum inspiratory mouth pressure (Pimax) (p = 0.01); strength-index (p = 0.02); peak inspiratory flow (PIF) (p = 0.02), with no evidence of change in spirometry, PECF or HRQoL. No adverse events occurred and participant satisfaction and adherence levels were high.

Conclusion: Inspiratory muscle training (at an intensity of 30% Pimax) appears safe, feasible and acceptable, in a small sample of children and adolescents with NMD and was associated with improved inspiratory muscle strength, PIF and upper limb function and coordination.

Clinical implications: Larger, longer-term randomised controlled trials are warranted to confirm the safety and efficacy of IMT as an adjunct respiratory management strategy in children with NMD.

Keywords: children; inspiratory muscle strength; inspiratory muscle training; neuromuscular disease; pulmonary function.

Conflict of interest statement

The authors declare that they have no financial or personal relationships that may have inappropriately influenced them in writing this article.

© 2021. The Authors.

Figures

FIGURE 1
FIGURE 1
The OMNI scale used for participants to describe their level of perceived exertion.
FIGURE 2
FIGURE 2
Mean sniff nasal inspiratory pressure change over training period (ANOVA, p = 0.39).
FIGURE 3
FIGURE 3
Mean maximum inspiratory pressure change over training period (ANOVA, p = 0.02).
FIGURE 4
FIGURE 4
Mean peak inspiratory flow change over training period (ANOVA, p = 0.007).

References

    1. Aboussouan, L., 2009, ‘Mechanisms of exercise limitation and pulmonary rehabilitation for patients with neuromuscular disease’, Chronic Respiratory Disease 6(4), 231–249. 10.1177/1479972309345927
    1. Aslan, G.K., Gurses, H.N., Issever, H. & Kiyan, E., 2013, ‘Effects of respiratory muscle training on pulmonary functions in patients with slowly progressive neuromuscular disease: A randomized controlled trial’, Clinical Rehabilitation 28(6), 573–581. 10.1177/0269215513512215
    1. Benditt, J.O., 2006, ‘The neuromuscular respiratory system: Physiology, pathophysiology, and a respiratory care approach to patients’, Respiratory Care 51(8), 829–839.
    1. Bianchi, C. & Baiardi, P., 2008, ‘Cough peak flows: Standard values for children and adolescents’, American Journal of Physical Medicine & Rehabilitation 87(6), 461–467. 10.1097/PHM.0b013e318174e4c7
    1. Birnkrant, D.J., Bushby, K., Bann, C.M., Alman, B.A., Apkon, S.D., Blackwell, A. et al. , 2018, ‘Diagnosis and management of Duchenne muscular dystrophy, part 2: Respiratory, cardiac, bone health, and orthopaedic management’, The Lancet Neurology 17(4), 347–361. 10.1016/S1474-4422(18)30025-5
    1. Boentert, M., Wenninger, S. & Sansone, V.A., 2017, ‘Respiratory involvement in neuromuscular disorders’, Current Opinion in Neurology 30(5), 529–537. 10.1097/WCO.0000000000000470
    1. Bushby, K. & Connor, E., 2011, ‘Clinical outcome measures for trials in Duchenne muscular dystrophy: Report from International working group meetings’, Clinical Investigation 1(9), 1217–1235. 10.4155/cli.11.113
    1. Caruso, P., De Albuquerque, A.L.P., Santana, P.V., Cardenas, L.Z., Ferreira, J.G., Prina, E. et al. . 2015, ‘Diagnostic methods to assess inspiratory and expiratory muscle strength’, Jornal Brasileiro de Pneumologia 41(2), 110–123. 10.1590/S1806-37132015000004474
    1. Chatwin, M., Ross, E., Hart, N., Nickol, A., Polkey, M. & Simonds, A., 2003, ‘Cough augmentation with mechanical insufflation/exsufflation in patients with neuromuscular weakness’, European Respiratory Journal 21(3), 502–508. 10.1183/09031936.03.00048102
    1. Chatwin, M., Toussaint, M., Gonçalves, M.R., Sheers, N., Mellies, U., Gonzales-Bermejo, J. et al. , 2018, ‘Airway clearance techniques in neuromuscular disorders: A state of the art review’, Respiratory Medicine 136, 98–110. 10.1016/j.rmed.2018.01.012
    1. Chiang, J., Mehta, K. & Amin, R., 2018, ‘Respiratory diagnostic tools in neuromuscular disease’, Children 5(6), 78. 10.3390/children5060078
    1. Eagle, M., 2002, ‘Report on the muscular dystrophy campaign workshop: Exercise in neuromuscular diseases Newcastle, January 2002’, Neuromuscular Disorders 12(10), 975–983. 10.1016/S0960-8966(02)00136-0
    1. European Respiratory Society , 2021, Global Lung Function Initiative 2021|Version 2.0., viewed 28 July 2021, from
    1. Farrero, E., Antón, A., Egea, C.J., Almaraz, M.J., Masa, J.F., Utrabo, I. et al. , 2013, ‘Guidelines for the management of respiratory complications in patients ith neuromuscular disease’, Archivos de Bronconeumologia 49(7), 306–313. 10.1016/j.arbres.2012.12.003
    1. Fauroux, B. & Aubertin, G., 2007, ‘Measurement of maximal pressures and the sniff manoeuvre in children’, Paediatric Respiratory Reviews 8(1), 90–93. 10.1016/j.prrv.2007.02.006
    1. Finder, J.D., Birnkrant, D., Carl, J., Farber, H.J., Gozal, D., Iannaccone S.T. et al. , 2004, ‘Respiratory care of the patient with Duchenne muscular dystrophy: ATS consensus statement’, American Journal of Respiratory and Critical Care Medicine 170(4), 456–465. 10.1164/rccm.200307-885ST
    1. Gozal, D., 2000, ‘Pulmonary manifestations of neuromuscular disease with special reference to Duchenne muscular dystrophy and spinal muscular atrophy’, Pediatric Pulmonology 29(2), 141–150. 10.1002/(SICI)1099-0496(200002)29:2<141::AID-PPUL9>;2-Y
    1. Gozal, D. & Thiriet, P., 1999, ‘Respiratory muscle training in neuromuscular disease: Long-term effects on strength and load perception’, Medicine and Science in Sports and Exercise 31(11), 1522–1527. 10.1097/00005768-199911000-00005
    1. Guglieri, M. & Bushby, K., 2011, ‘Recent developments in the management of Duchenne muscular dystrophy’, Paediatrics and Child Health 21(11), 501–509. 10.1016/j.paed.2011.06.007
    1. Hill, K., Cecins, N.M., Eastwood, P.R. & Jenkins, S.C., 2010, ‘Inspiratory muscle training for patients with chronic obstructive pulmonary disease: A practical guide for clinicians’, Archives of Physical Medicine and Rehabilitation 91(9), 1466–1470. 10.1016/j.apmr.2010.06.010
    1. Hull, J., Aniapravan, R., Chan, E., Chatwin, M., Forton, J., Gallagher, J. et al. , 2012, ‘BTS guideline for respiratory management of children with neuromuscular weakness’, Thorax 67(Suppl 1), i1–i40. 10.1136/thoraxjnl-2012-201964
    1. Human, A., Corten, L., Jelsma, J. & Morrow, B., 2017, ‘Inspiratory muscle training for children and adolescents with neuromuscular diseases: A systematic review’, Neuromuscular Disorders 27(6), 503–517. 10.1016/j.nmd.2017.03.009
    1. Human, A., Corten, L. & Morrow, B., 2021, ‘The role of physiotherapy in the respiratory management of children with neuromuscular diseases: A South African perspective’, South African Society of Physiotherapy Journal 77(1), a1527. 10.4102/sajp.v77i1.1527
    1. Human, A., Honey, E. & Morrow, B., 2019, ‘Inspiratory muscle training in severe spinal muscular atrophy: A case report’, International Journal of Therapy and Rehabilitation 26(4), 1–19. 10.12968/ijtr.2017.0108
    1. Iannaccone, S.T., Hynan, L.S., Morton, A., Buchanan, R., Limbers, C.A. & Varni, J.W., 2009, ‘The PedsQLTM in pediatric patients with spinal muscular atrophy: Feasibility, reliability, and validity of the pediatric quality of life inventoryTM generic core scales and neuromuscular module’, Neuromuscular Disorders 19(12), 805–812. 10.1016/j.nmd.2009.09.009
    1. Iwabe, C., Nucci, A., Pfeilsticker, B.H.M. & Magna, L.A., 2014, ‘Chapter 16: Motor function measure scale (MFM): New instrument for follow-up Brazilian patients with neuromuscular disease’, viewed n.d., from
    1. Kinane, T.B., Mayer, O.H., Duda, P.W., Lowes, L.P., Moody, S.L. & Mendell, J.R., 2017, ‘Long-term pulmonary function in Duchenne muscular dystrophy: Comparison of eteplirsen-treated patients to natural history’, Journal of Neuromuscular Diseases 5(1), 47–58. 10.3233/JND-170272
    1. Koessler, W., Wanke, T., Winkler, G., Nader, A., Toifl, K., Kurz, H. et al. , 2001, ‘2 years’ experience with inspiratory muscle training in patients with neuromuscular disorders’, CHEST Journal 120(3), 765–769. 10.1378/chest.120.3.765
    1. Lӧtters, F., Van Tol, B., Kwakkel, G. & Gosselink, R., 2002, ‘Effects of controlled inspiratory muscle training in patients with COPD: A meta-analysis’, European Respiratory Journal 20(3), 570–577. 10.1183/09031936.02.00237402
    1. Lue, Y.-J., Lin, R.-F., Chen, S.-S. & Lu, Y.-M., 2009, ‘Measurement of the functional status of patients with different types of muscular dystrophy’, The Kaohsiung Journal of Medical Sciences 25(6), 325–333. 10.1016/S1607-551X(09)70523-6
    1. Marques, T.B.C., Neves, C., Portes, L.A., Salge, J.M., Zanoteli, E. & Reed, U.C., 2014, ‘Air stacking: Effects on pulmonary function in patients with spinal muscular atrophy and in patients with congenital muscular dystrophy’, Jornal Brasileiro de Pneumologia 40(5), 528–534. 10.1590/S1806-37132014000500009
    1. Mayer, O.H., Henricson, E.K., McDonald, C.M. & Buyse, G.M., 2017, ‘Advances in pulmonary care in Duchenne muscular dystrophy’, US Neurology 13(1), 35–41. 10.17925/USN.2017.13.01.35
    1. Mazzone, E.S., Vasco, G., Palermo, C., Bianco, F., Galluccio, C., Ricotti, V. et al. , 2012, ‘A critical review of functional assessment tools for upper limbs in Duchenne muscular dystrophy’, Developmental Medicine and Child Neurology 54(10), 879–885. 10.1111/j.1469-8749.2012.04345.x
    1. McCool, F.D. & Tzelepis, G.E., 1995, ‘Inspiratory muscle training in the patient with neuromuscular disease’, Physical Therapy 75(11), 1006–1014. 10.1093/ptj/75.11.1006
    1. Meier, T., Rummey, C., Leinonen, M., Spagnolo, P., Mayer, O.H., Buyse, G.M. et al. , 2017, ‘Characterization of pulmonary function in 10–18 year old patients with Duchenne muscular dystrophy’, Neuromuscular Disorders 27(4), 307–314. 10.1016/j.nmd.2016.12.014
    1. Miller, M.R., Hankinson, J., Brusasco, V., Burgos, F., Casaburi, R., Coates, A. et al. , 2005, ‘Standardisation of spirometry’, European Respiratory Journal 26(2), 319–338. 10.1183/09031936.05.00034805
    1. Morrow, B.M., 2019, ‘Airway clearance therapy in acute paediatric respiratory illness: A state-of-the-art review’, South African Journal of Physiotherapy 75(1), a1295. 10.4102/sajp.v75i1.1295
    1. Motor Function Measure (MFM) user manual , viewed 29 July 2021, from
    1. Nicot, F., Hart, N., Forin, V., Boulé, M., Clément, A., Polkey, M.I. et al. , 2006, ‘Respiratory muscle testing: A valuable tool for children with neuromuscular disorders’, American Journal of Respiratory and Critical Care Medicine 174(1), 67–74. 10.1164/rccm.200512-1841OC
    1. Park, J.H., Kang, S.-W., Lee, S.C., Choi, W.A. & Kim, D.H., 2010, ‘How respiratory muscle strength correlates with cough capacity in patients with respiratory muscle weakness’, Yonsei Medical Journal 51(3), 392–397. 10.3349/ymj.2010.51.3.392
    1. Sander, M., Chavoshan, B., Harris, S.A., Iannaccone, S.T., Stull, J.T., Thomas, G.D. et al. , 2000, ‘Functional muscle ischemia in neuronal nitric oxide synthase-deficient skeletal muscle of children with Duchenne muscular dystrophy’, Proceedings of the National Academy of Sciences 97(25), 13818–13823. 10.1073/pnas.250379497
    1. Silva, I.S., Pedrosa, R., Azevedo, I.G., Forbes, A.-M., Fregonezi, G.A., Junior, M.E.D. et al. , 2019, ‘Respiratory muscle training in children and adults with neuromuscular disease’, Cochrane Database of Systematic Reviews 9(9), CD011711. 10.1002/14651858.CD011711.pub2
    1. Statistics How To , 2021, Cohen’s D: Definition, Examples, Formula, viewed 28 July 2021, from
    1. Stefanutti, D., Benoist, M.R., Scheinmann, P., Chaussain, M. & Fitting, J.W., 2000, ‘Usefulness of sniff nasal pressure in patients with neuromuscular or skeletal disorders’, American Journal of Respiratory and Critical Care Medicine 162(4), 1507–1511. 10.1164/ajrccm.162.4.9910034
    1. Tidball, J.G. & Wehling-Henricks, M., 2014, ‘Nitric oxide synthase deficiency and the pathophysiology of muscular dystrophy’, The Journal of Physiology 592(21), 4627–4638. 10.1113/jphysiol.2014.274878
    1. Tomalak, W., Pogorzelski, A. & Prusak, J., 2002, ‘Normal values for maximal static inspiratory and expiratory pressures in healthy children’, Pediatric Pulmonology 34(1), 42–46. 10.1002/ppul.10130
    1. Topin, N., Matecki, S., Le Bris, S., Rivier, F., Echenne, B., Prefaut, C. et al. , 2002, ‘Dose-dependent effect of individualized respiratory muscle training in children with Duchenne muscular dystrophy’, Neuromuscular Disorders 12(6), 576–583. 10.1016/S0960-8966(02)00005-6
    1. Toussaint, M., Chatwin, M., Gonzales, J., Berlowitz, D.J. & ENMC Respiratory Therapy Consortium , 2018, ‘228th ENMC International Workshop: Airway clearance techniques in neuromuscular disorders Naarden, The Netherlands, 3–5 March, 2017’, Neuromuscular Disorders 28(3), 289–298. 10.1016/j.nmd.2017.10.008
    1. Varni, J.W., Seid, M. & Kurtin, P.S., 2001, ‘PedsQLTM 4.0: Reliability and validity of the pediatric quality of life inventoryTM version 4.0 generic core scales in healthy and patient populations’, Medical Care 39(8), 800–812. 10.1097/00005650-200108000-00006
    1. Verma, R., Chiang, J., Qian, H. & Amin, R., 2019, ‘Maximal static respiratory and sniff pressures in healthy children: A systematic review and meta-analysis’, Annals of the America Thoracic Society 16(4), 478–487. 10.1513/AnnalsATS.201808-506OC
    1. Wanke, T., Toifl, K., Merkle, M., Formanek, D., Lahrmann, H. & Zwick, H., 1994, ‘Inspiratory muscle training in patients with Duchenne muscular dystrophy’, CHEST Journal 105(2), 475–482. 10.1378/chest.105.2.475
    1. Winkler, G., Zifko, U., Nader, A., Frank, W., Zwick, H., Toifl, K. et al. , 2000, ‘Dose-dependent effects of inspiratory muscle training in neuromuscular disorders’, Muscle & Nerve: Official Journal of the American Association of Electrodiagnostic Medicine 23(8), 1257–1260. 10.1002/1097-4598(200008)23:8<1257::AID-MUS15>;2-M
    1. Yeldan, I., Gurses, H.N. & Yuksel, H., 2008, ‘Comparison study of chest physiotherapy home training programmes on respiratory functions in patients with muscular dystrophy’, Clinical Rehabilitation 22(8), 741–748. 10.1177/0269215508091203

Source: PubMed

3
Suscribir